Production Engineer II, Medical Devices & Lean

Getinge Group; Merrimack (NH); On-site; USD 75,000 - 100,000; Full time

Benefits offered by this job

Health, Dental, and Vision insurance

401k plan with company match

Paid Time Off

Wellness initiative

Life Insurance

Disability Benefits

Flexible Spending Accounts

Parental and Caregiver Leave

Tuition Reimbursement

Job summary

Atrium Medical Corporation in Merrimack, NH is seeking a manufacturing/quality engineer to support the commercialized production of medical devices. You will contribute to quality, process development, continuous improvement, and process control in a hands-on team environment.

Responsibilities include supporting production, leading lean initiatives, developing work instructions, performing validation (IQ/OQ/PQ), CAPA and non-conformance investigations, and data analysis.

Qualifications

• Bachelor’s Degree in Engineering and three years related manufacturing experience (medical device field preferred).
• Must be highly skilled in equipment troubleshooting (electro-mechanical) and data analysis.
• Demonstrated knowledge of MS Office applications; Minitab experience preferred.

Responsibilities

• Supports production/manufacturing and Lean initiatives.
• Develops work instructions and training for transfer into production.
• Performs process development and validation (IQ, OQ, PQ, EAT, TMV).
• Leads CAPA, non-conformance investigations, PFMECA’s, MES, and equipment troubleshooting.
• Executes ECOs related to process and equipment documentation.
• Performs data analysis and root cause investigations.

Skills

Equipment troubleshooting (Electro-mec

Problem solving

Data analysis

MS Office (Word/Excel/PPT)

Minitab experience

Education

Bachelor’s Degree in Engineering or equivalent

Tools

CAD / SolidWorks

Job description

Atrium Medical Corporation in Merrimack, NH is seeking a manufacturing/quality engineer to support the commercialized production of medical devices. You will contribute to quality, process development, continuous improvement, and process control in a hands-on team environment.

Responsibilities include supporting production, leading lean initiatives, developing work instructions, performing validation (IQ/OQ/PQ), CAPA and non-conformance investigations, and data analysis.